Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.02 (C)
Location

Chromosome 5:181236549 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

5:g.181236549A>C

About this variant

This variant overlaps 42 transcripts and has 2505 sample genotypes.

Variant displays